Wolcott-Rallison syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Genetics(clinical),General Medicine
Link
http://link.springer.com/content/pdf/10.1186/1750-1172-5-29.pdf
Reference45 articles.
1. Wolcott CD, Rallison MV: Infancy-onset diabetes mellitus and multiple epiphyseal dysplasia. J Pediatr. 1972, 80: 292-297. 10.1016/S0022-3476(72)80596-1.
2. Senee V, Vattem KM, Delepine M, Rainbow LA, Haton C, Lecoq A, Shaw NJ, Robert JJ, Rooman R, Diatloff-Zito C: Wolcott-Rallison Syndrome: Clinical, Genetic, and Functional Study of EIF2AK3 Mutations and Suggestion of Genetic Heterogeneity. Diabetes. 2004, 53: 1876-1883. 10.2337/diabetes.53.7.1876.
3. Ozbek MN, Senée V, Aydemir S, Kotan LD, Mungan NO, Yuksel B, Julier C, Topaloglu AK: Wolcott-Rallison syndrome due to the same mutation (W522X) in EIF2AK3 in two unrelated families and review of the literature. Pediatric Diabetes. 2010, 11: 279-285. 10.1111/j.1399-5448.2009.00591.x.
4. Rubio-Cabezas O, Patch AM, Minton JA, Flanagan SE, Edghill EL, Hussain K, Balafrej A, Deeb A, Buchanan CR, Jefferson IG: Wolcott-Rallison syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous families. J Clin Endocrinol Metab. 2009, 94: 4162-4170. 10.1210/jc.2009-1137.
5. Al-Gazali LI, Makia S, Hall CM: Wolcott-Rallison syndrome. Clinical Dysmorphology. 1995, 4: 227-233. 10.1097/00019605-199507000-00006.
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